The preparation and isolation of the metalated ylides [Cy3PCSO2Tol]M (Cy1-M) (with M = Li, Na, K) are reported. In contrast to its triphenylphosphonium analogue the synthesis of Cy1-M revealed to be less straight forward. Synthetic routes to the phosphonium salt precursor Cy1-H2 via different methods revealed to be unsuccessful or low-yielding. However, nucleophilic attack of the ylide Cy3P = CH2 at toluenesulfonyl fluoride under basic conditions proved to be a high-yielding method directly leading to the ylide Cy1-H. Metalation to the yldiides was finally achieved with strong bases such as nBuLi, NaNH2, or BnK. In the solid state, the lithium compound forms a tetrameric structure consisting of a (C–S–O–Li)4 macrocycle, which incorporates an additional molecule of lithium iodide. The potassium compound forms a C4-symmetric structure with a (K4O4)2 octahedral prism as central structural motif. Upon deprotonation the P–C–S linkage undergoes a remarkable contraction typical for metalated ylides.
CITATION STYLE
Darmandeh, H., Scherpf, T., Feichtner, K. S., Schwarz, C., & Gessner, V. H. (2020). Synthesis, Isolation and Crystal Structures of the Metalated Ylides [Cy3P-C-SO2Tol]M (M = Li, Na, K). Zeitschrift Fur Anorganische Und Allgemeine Chemie, 646(13), 835–841. https://doi.org/10.1002/zaac.201900333
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